Canonical Allele Identifier: CA691232941
Gene: IFNG HGNC NCBI

Linked Data

dbSNP Id: rs34079299
gnomAD v3: 12-68158714-AGTGTGTGT-A
gnomAD v4: 12-68158714-AGTGTGTGT-A
MyVariant Identifiers: chr12:g.68552495_68552502del (hg19) chr12:g.68158715_68158722del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68158736_68158743del , CM000674.2:g.68158736_68158743del GRCh38
NC_000012.11:g.68552516_68552523del , CM000674.1:g.68552516_68552523del GRCh37
NC_000012.10:g.66838783_66838790del NCBI36
NG_015840.1:g.6020_6027del

Transcript Alleles

HGVS Amino-acid change
ENST00000229135.4:c.115-463_115-456del MANE Select ENSP00000229135.3:n.115-463_115-456del
ENST00000229135.3:c.115-463_115-456del ENSP00000229135.3:n.115-463_115-456del
NM_000619.2:c.115-463_115-456del NP_000610.2:n.115-463_115-456del
NM_000619.3:c.115-463_115-456del MANE Select NP_000610.2:n.115-463_115-456del
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Search 100 bp 3'